ETMExperimental and Therapeutic Medicine1792-09811792-1015D.A. Spandidos10.3892/etm.2012.518etm-03-06-0931ArticlesMembranous and cytoplasmic expression of epidermal growth factor receptor in metastatic pancreatic ductal adenocarcinomaEINAMATAKAHIRO16UEDASHIGETO2TSUDAHITOSHI37OGASAWARAKAZUHIRO5HATSUSEKAZUO4MATSUBARAOSAMU3TODOSATORU1YAMAMOTOJUNJI4
Department of General Surgery, Hokkaido University, Graduate School of Medicine, Sapporo;
Medical Service School, National Defense Force, Tokyo;
Departments of Basic Pathology and
Surgery, National Defense Medical College, Saitama;
Department of Surgery, Japan Labor Health and Welfare Organization Kushiro Rosai Hospital, Kushiro, Hokkaido;
Division of Gastroenterological and General Surgery, Department of Surgery, Asahikawa Medical University, Hokkaido,
JapanCorrespondence to: Dr Hitoshi Tsuda
Present address: Pathology Section, Clinical Laboratory Division, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan E-mail: hstsuda@ncc.go.jp
Recent studies indicate the clinical significance of the cellular localization of epidermal growth factor receptor (EGFR) in a variety of cancer types. Internalization of activated EGFR is reported to be closely associated with patient prognosis. This study investigated the clinical significance of the immunohistochemical localization of EGFR in patients with metastatic pancreatic cancers compared to those with surgically resected pancreatic cancers. Using 44 surgically resected primary pancreatic cancers and 40 primary or meta-static tumors from 20 autopsied patients with far advanced pancreatic cancers, the incidence of membranous and cytoplasmic EGFR overexpression was compared between primary tumors and far advanced tumors by immunohistochemistry using the Dako EGFR pharmDx™ kit, a global standard kit for EGFR assay. In the 44 surgically resected cancers, 13 (30%) exhibited membranous overexpression of EGFR, comprising 1 case (2%) with score 3+ and 12 cases (27%) with score 2+ and 10 (23%) exhibited cytoplasmic overexpression of EGFR. In the 40 tumors at a far advanced stage, the percentage of samples exhibiting positivity for membranous and cytoplasmic EGFR overexpression was 48% (19 of 40) comprising 7 (18%) with score 2+ and 12 (30%) with score 3+ and 33% (13 of 40), respectively. The far advanced tumors tended to show membranous and cytoplasmic EGFR overexpression more frequently than the surgically resected tumors, although the difference was not significant. These findings suggest that membranous and cytoplasmic overexpression of EGFR may be indicative of the potential aggressiveness of pancreatic cancers.
Despite recent advances in diagnostic and therapeutic techniques, pancreatic carcinoma is one of the most lethal malignancies among cancers. The 5-year survival rate of patients having primary pancreatic cancer after complete resection does not reach 15% (1), while the overall 5-year survival rates in patients having inoperable pancreatic cancer are desperately low, ranging from 0.4 to 4% (2,3).
Currently, gemcitabine is a key drug not only for treating advanced pancreatic cancer (4) but also as an adjuvant chemotherapy regimen for resectable pancreatic cancer (5,6). Furthermore, molecular targeting of epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) has recently been developed to treat these lesions (7,8). Moore et al reported in a phase III trial of patients with advanced pancreatic cancer, that erlotinib, a tyrosine kinase inhibitor of EGFR, in combination with gemcitabine was superior to gemcitabine alone when progression-free and overall survival were compared between the two groups (8).
EGFR, one of the tyrosine kinase receptors of the ErbB family, is reported to be expressed immunohistochemically in 10–30% of patients with solid tumors including pancreatic carcinoma (9,10). Tyrosine phosphorylation in EGFR protein in cancer cells leads to activation of several downstream intra cellular substrates and plays a pivotal role in tumor proliferation, invasion and metastasis (11). Recent studies have suggested that the EGFR gene copy number and expression obtained by fluorescence in situ hybridization (FISH) and immunohisto chemistry (IHC) predict the clinical response of a tumor to gefitinib, a tyrosine kinase inhibitor of EGFR, in patients with non-small cell lung cancer (12–14). Furthermore, recent studies have found that mutations of the EGFR gene at the restricted region, e.g., exon 19 and exon 21, were closely correlated with response to gefitinib therapy (15–20). However, the relevance of EGFR expression in pancreatic cancer with therapeutic response has remained to be verified (8).
Although immunohistochemical expression of EGFR can also be recognized as positive membranous staining, cytoplasmic expression of EGFR can frequently be observed in cancer cells of the pancreas. We previously reported that high cytoplasmic expression of EGFR in primary pancreatic cancer was significantly correlated with higher histological grade and poorer survival (10), suggesting that cytoplasmic EGFR expression could indicate a potentially aggressive or metastatic feature of pancreatic cancer. However, it is unclear whether localization of EGFR expression differs between primary and metastatic sites of pancreatic cancers at surgically resectable stages and those at inoperable far advanced stages.
The present study compared immunohistochemically the levels and localization of EGFR expression between surgically resected primary pancreatic cancers and far advanced cancers obtained at autopsy, in order to clarify the clinical impact of membranous and cytoplasmic EGFR overexpressions in far advanced pancreatic cancers.
Materials and methodsPatients and tumor specimens
This study was performed with approval by the Internal Review Board on Ethical Issues of the National Defense Medical College, Japan. The subjects of this study were 44 patients who underwent surgery with curative intent for primary pancreatic cancers between 1987 and 2000 at the National Defense Medical College Hospital, Tokorozawa, Japan. The clinicopathological characteristics of these cases are summarized in Table I.
The mean patient age was 63.3 years [±3.7 standard deviation (SD)]. Thirty-four (77.3%) were men and 10 (22.7%) were women. More than 80% of tumors were located in the head of the pancreas. As for stage, approximately 90% of the patients were assigned to stage II or stage III (21). Histologically, all 44 patients had invasive ductal adenocarcinoma of the pancreas, and the majority of the patients had moderately differentiated tubular adenocarcinoma. The median survival time was 24.5 months (±10.3 SD).
In addition, a total of 40 tumor specimens from primary sites and hepatic metastatic sites were obtained at autopsy from 20 patients who had died of inoperable far advanced pancreatic cancer between 1980 and 2001 at the same hospital (Table I).
Using these tumor specimens from a total of 64 patients, formalin-fixed paraffin-embedded tissue blocks were prepared, and sections were cut and stained with hematoxylin and eosin (H&E) for routine histopathological examination. Because surgically resected specimens had been cut routinely for pathology specimens once a weak periodically, the duration of formalin fixation of the surgically resected specimens varied from 1 to 6 days. Likewise, the duration of formalin fixation of the autopsied tissues varied from 1 to 6 days. All specimens were diagnosed as ductal adenocarcinomas of the pancreas. After a histological review of the sections by three observers (T.E., H.T. and S.U.), a representative tissue block was selected from each surgically resected primary tumor, each primary tumor obtained by autopsy, and each metastatic tumor obtained by autopsy. These tumor tissue blocks were subjected to immuno histochemical studies.
Histological classification
The three observers graded the degree of tumor differentiation. Tumor differentiation was classified into Grade 1 (well-differentiated type), Grade 2 (moderately differentiated type) and Grade 3 (poorly differentiated type), according to the degree of tubular formation (21). The grade of each primary cancer was defined according to the findings in the widest area of the representative section of the cancer.
Immunohistochemistry
Immunohistochemical staining for EGFR was performed using the EGFR pharmDx™ kit (Dako, Carpinteria, CA, USA), a global standard kit for EGFR assay approved by the US Food and Drug Administration (US FDA). Sections were deparaffinized in two sequential xylene baths (5 min), 100% ethanol (3 min) and 95% ethanol (3 min), followed by a 5-min single wash in wash-buffer solution (Dako). Subsequently, at room temperature, the section was rinsed in wash-buffer for 5 min, incubated in proteinase K solution (Dako) for 5 min, rinsed again in the wash-buffer for 5 min, incubated in peroxidase blocking agent for 5 min, rinsed, incubated with the primary EGFR antibody or negative control reagent for 30 min, rinsed, incubated with visualization reagent for 30 min, rinsed twice with the buffer, incubated with substrate chromogen solution for 5 min and finally rinsed again with the buffer. Slides were counterstained with hematoxylin and rinsed gently in reagent quality water. The positive and negative controls used were formalin-fixed, paraffin-embedded pellets of HT-29 and CAMA-1 cell lines, which expressed and did not express EGFR, respectively (Dako).
Immunohistochemical evaluation
Immunohistochemical evaluation was performed for both the cell membrane and cytoplasm, separately, for the primary or metastatic carcinoma samples. The level of membranous EGFR expression was stratified into 4 groups (scores 0, 1+, 2+ and 3+) according to the criteria for the HER2 test (HercepTest) (22). In detail, when membranous staining was observed in <10% of the tumor cells, a score of 0 was assigned, regardless of the intensity of the staining. If faint or barely perceptible membranous staining was detected in >10% of the tumor cells, a score of 1+ was assigned. Scores of 2+ and 3+ were assigned when weak to moderate staining and strong staining, respectively, were observed on the entire membrane in >10% of the tumor cells (Fig. 1). Cases showing a score of 2+ or 3+ were defined as showing overexpression.
Cytoplasmic staining was divided into 3 grades (0, 1+ and 2+), as grading of the intensity of the immunoreaction was difficult for the cytoplasm. The level of cytoplasmic staining was categorized as follows: when cytoplasmic staining was observed in <10% of the tumor cells, a score of 0 was assigned. If faint or barely perceptible cytoplasmic staining was detected in >10% of tumor cells, a score of 1+ was assigned. A score of 2+ was assigned when moderate or strong staining, respectively, was observed in >10% of the tumor cells. Cytoplasmic granular staining was also scored as 2+. Cases showing a score of 2+ were judged as showing overexpression (Fig. 2).
Statistical analysis
We used the χ2 test or Fisher’s exact test to determine the correlation between EGFR expression and histological grade. Differences were considered to indicate statistical significance at a P-value <0.05. All statistical analyses were performed using Statview 5.0 software (SAS Institute Inc., Cary, NC, USA).
Results
The expression profiles of membranous and cytoplasmic EGFR in both surgically resected cancers and far advanced cancers obtained at autopsy are shown in Table II. In the 44 surgically resected cancers, 13 (30%) exhibited membranous overexpression of EGFR, comprising 1 case (2%) of score 3+ and 12 cases (27%) of score 2+ and 10 (23%) exhibited cytoplasmic overexpression of EGFR.
In the primary tumors in the 20 far advanced cancers, the percentage of samples with positivity for membranous EGFR overexpression was 40%, (8 of 20), comprising 3 cases (15%) of score 2+ and 5 cases (25%) of score 3+, and the percentage of samples showing positivity for cytoplasmic EGFR overexpresion was 25% (5 of 20). In the hepatic metastases in the 20 far advanced cancers, the positivity of membrane EGFR overexpression was 55%, (11 of 20), comprising 4 cases (20%) of score 2+ and 7 cases (35%) of score 3+, and the positivity of cytoplasmic EGFR overexpresion was 40% (8 of 20).
In a total of 40 tumors at a far advanced stage, the percentage of samples showing positivity for membranous EGFR over-expression was 48% (19 of 40) comprising 7 cases (18%) of score 2+ and 12 cases (30%) of score 3+, and the percentage of samples showing positivity for cytoplasmic EGFR overexpresion was 33% (13 of 40). Therefore, the far advanced tumors tended to show membranous and cytoplasmic EGFR overexpression more frequently than the surgically resected tumors, although the difference was not significant.
When these cases were stratified according to histological grade, higher grade (Grades 2 and 3) cancer tissues tended to show membranous EGFR overexpression more frequently (12 of 32, 38%) than the lower grade (Grade 1) cancer tissues (1 of 12, 8%) in the surgically resected pancreatic cancers, although the difference was statistically marginal (P= 0.07). The percentage of cytoplasmic EGFR overexpression did not differ statistically between the low grade (Grade 1) tumors (1 of 12, 8%) and higher grade (Grades 2 and 3) tumors (9 of 32, 28%) in the surgically resected cases.
The tissues of the far advanced cancers showed similar rates of membranous and cytoplasmic overexpressions, regardless of histological grade. In the 40 far advanced tumors, membranous EGFR overexpression was detected in 3 (43%) of 7 Grade 1 cases and in 16 (48%) of Grade 2 or 3 cases. In these far advanced tumors, cytoplasmic overexpression of EGFR was detected in 14% (1 of 7) of Grade 1 tumors and 36% (12 of 33) of Grade 2 or 3 tumors (Table III).
Discussion
In the present study, we demonstrated that EGFR overexpression in the cell membrane and cytoplasm was common in both surgically resected and far advanced pancreatic carcinomas. The occurrences of membranous and cytoplasmic EGFR over-expression tended to be higher in the tumors at far advanced stages than in the tumors that were at surgically resectable stages as determined using a global standard kit for EGFR assay.
Cytoplasmic EGFR expression in the far advanced cancers may be explained by the hypothesis of epithelial-to-mesenchymal transition which is thought be an important mechanism for promoting cancer invasion and metastasis (23). Persistently activated EGFR can decrease intercellular adhesion between tumor cells and enhance cancer cell migration. Willmarth et al showed that EGF-activated EGFR in MCF10A cells enhanced signal transduction predominantly from the endosomes rather than from the membrane (24). Barr et al (25) suggested that continuously EGF-treated EGFR induced endocytosis of E-cadherin, a cell-to-cell adhesion protein, which enhanced invasiveness in several human cancer cell lines. Ueda et al previously reported that EGFR overexpression in the cytoplasm of pancreatic cancers was associated with poorer clinical outcome of patients (10,26). The present study corroborated that not only membranous overexpression but also cytoplasmic overexpression of EGFR is important for the acquisition of highly aggressive and metastatic properties of pancreatic carcinomas.
In the present study, the rate of EGFR overexpression in surgically resected cancers tended to be higher in higher grade (Grades 2 and 3) tumors than in low grade (Grade 1) tumors. It is not surprising that poorly differentiated pancreatic cancers exhibited a higher incidence of EGFR overexpression as the patients with pancreatic carcinoma with altered EGFR activity tend to show a more aggressive clinical course and a poorer clinical outcome (27). Aggressive tumors appear to require the activation of an EGFR-mediated autocrine signaling in order to maintain proliferation. Therefore, we suppose the possibility that cytoplasmic EGFR protein, which is newly synthesized within the endoplasm reticulum, would be processed at the cellular surface. Some investigators reported that binding of EGF to EGFR activates its receptor tyrosine kinases and accelerates its internalization through clathrin-coated pits followed by the efficient lysosomal targeting of internalized receptors, which results in receptor downregulation and degradation. Thus, the ligand-induced internalization of EGFR, so-called endocytosis trafficking, is characterized as activated EGFR (28–30). If the EGFR ligands dissociated EGFR localized in endosomes, EGFR would be deactivated and recycled to the plasma membrane.
We should consider the possibility that EGFR localization and its activity in advanced or metastatic pancreatic cancers may be modulated by chemotherapy or radiation therapy which those patients had received. It is known that ionizing radiation, hypoxia and oxidative stress can also phosphorylate EGFR with ligand independence, which is sequentially internalized and shuttled into the nucleus (31). Li et al (32) reported that the non-small cell lung cancer H226 cells which acquire resistance to cetuximab, an anti-EGFR antibody, showed decreased membranous EGFR accompanied by EGFR expressed with nuclear localization. These findings imply that EGFR localization of cancer cells may be an important determinant of responsiveness to specific therapies.
In conclusion, we demonstrated using immunohistochemistry that membranous and cytoplasmic EGFR overexpression was frequently noted in surgically resected and far advanced pancreatic cancers. These findings suggest that membranous and cytoplasmic overexpression of EGFR may be indicative of the potential aggressiveness of pancreatic cancers.
This study was supported in part by a grant-in-aid for defense medicine from the Ministry of Defense and a grant-in-aid from the Foundation for Promotion of Defense Medicine. The authors thank Dr Tatsuro Takahashi and Mr. Ryuji Saito, Department of Central Laboratory, Japan Labor Health and Welfare Organization Kushiro Rosai Hospital, Kushiro, Hokkaido, Japan, for technical assistance with the immunohistochemistry.
ReferencesMatsunoSEgawaSFukuyamaSPancreatic Cancer Registry in Japan: 20 years of experiencePancreas282192302004BramhallSRAllumWHJonesAGAllwoodACumminsCNeoptolemosJPTreatment and survival in 13,560 patients with pancreatic cancer, and incidence of the disease, in the West Midlands: an epidemiological studyBr J Surg821111151995ParkinDMBrayFIDevesaSSCancer burden in the year 2000. The global pictureEur J Cancer37Suppl 8S4S662001BurrisHAIIIMooreMJAndersenJImprovements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trialJ Clin Oncol15240324131997OettleHPostSNeuhausPAdjuvant chemotherapy with gemcitabine vs observation in patients undergoing curative-intent resection of pancreatic cancer: a randomized controlled trialJAMA2972672772007UenoHKosugeTMatsuyamaYA randomised phase III trial comparing gemcitabine with surgery-only in patients with resected pancreatic cancer: Japanese Study Group of Adjuvant Therapy for Pancreatic CancerBr J Cancer1019089152009KindlerHLFribergGSinghDAPhase II trial of bevacizumab plus gemcitabine in patients with advanced pancreatic cancerJ Clin Oncol23803380402005MooreMJGoldsteinDHammJErlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials GroupJ Clin Oncol25196019662007SalomonDSBrandtRCiardielloFNormannoNEpidermal growth factor-related peptides and their receptors in human malignanciesCrit Rev Oncol Hematol191832321995UedaSOgataSTsudaHThe correlation between cytoplasmic overexpression of epidermal growth factor receptor and tumor aggressiveness: poor prognosis in patients with pancreatic ductal adenocarcinomaPancreas29e1e82004MendelsohnJBaselgaJStatus of epidermal growth factor receptor antagonists in the biology and treatment of cancerJ Clin Oncol21278727992003CappuzzoFHirschFRRossiEEpidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small cell lung cancerJ Natl Cancer Inst976436552005HirschFRVarella-GarciaMMcCoyJIncreased epidermal growth factor receptor gene copy number detected by fluorescence in situ hybridization associates with increased sensitivity to gefitinib in patients with bronchioloalveolar carcinoma subtypes: a Southwest Oncology Group StudyJ Clin Oncol23683868452005TsaoMSSakuradaACutzJCErlotinib in lung cancer – molecular and clinical predictors of outcomeN Engl J Med3531331442005LynchTJBellDWSordellaRActivating mutations in the epidermal growth factor receptor underlying responsiveness of non-small cell lung cancer to gefitinibN Engl J Med350212921392004HanSWKimTYHwangPGPredictive and prognostic impact of epidermal growth factor receptor mutation in non-small cell lung cancer patients treated with gefitinibJ Clin Oncol23249325012005MitsudomiTKosakaTEndohHMutations of the epidermal growth factor receptor gene predict prolonged survival after gefitinib treatment in patients with non-small cell lung cancer with postoperative recurrenceJ Clin Oncol23251325202005PaezJGJannePALeeJCEGFR mutations in lung cancer: correlation with clinical response to gefitinib therapyScience304149715002004TakanoTOheYSakamotoHEpidermal growth factor receptor gene mutations and increased copy numbers predict gefitinib sensitivity in patients with recurrent non-small cell lung cancerJ Clin Oncol23682968372005TakanoTOheYTsutaKEpidermal growth factor receptor mutation detection using high-resolution melting analysis predicts outcomes in patients with advanced non-small cell lung cancer treated with gefitinibClin Cancer Res13538553902007SobinLHWittekindChInternational Union Against Cancer (UICC) TNM Classification of Malignant Tumors6th editionWiley-LissNew York2002TsudaHAkiyamaFTerasakiHDetection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma. Interobserver reproducibility and correlation with immunohistochemical HER-2 overexpressionCancer92296529742001DembinskiJLKraussSCharacterization and functional analysis of a slow cycling stem cell-like subpopulation in pancreas adenocarcinomaClin Exp Metastasis266116232009WillmarthNEBailloADziubinskiMLWilsonKRieseDJIIEthierSPAltered EGFR localization and degradation in human breast cancer cells with an amphiregulin/EGFR autocrine loopCell Signal212122192009BarrSThomsonSBuckEBypassing cellular EGF receptor dependence through epithelial-to-mesenchymal-like transitionsClin Exp Metastasis256856932008UedaSHatsuseKTsudaHPotential crosstalk between insulin-like growth factor receptor type 1 and epidermal growth factor receptor in progression and metastasis of pancreatic cancerMod Pathol197887962006HolbroTCivenniGHynesNEThe ErbB receptors and their role in cancer progressionExp Cell Res284991102003MadshusIHStangEInternalization and intracellular sorting of the EGF receptor: a model for understanding the mechanisms of receptor traffickingJ Cell Sci122343334392009SorkinAGohLKEndocytosis and intracellular trafficking of ErbBsExp Cell Res3156836962009SorkinAvon ZastrowMEndocytosis and signalling: intertwining molecular networksNat Rev Mol Cell Biol106096222009DittmannKMayerCKehlbachRRodemannHPRadiation-induced caveolin-1 associated EGFR internalization is linked with nuclear EGFR transport and activation of DNA-PKMol Cancer7692008LiCIidaMDunnEFNuclear EGFR contributes to acquired resistance to cetuximabOncogene28380138132009Figures and Tables
Representative cases of pancreatic ductal adenocarcinoma showing scores of 1+, 2+ and 3+ for membranous EGFR expression. (A) Score 1+, incomplete membrane staining is weakly visible. (B) Score 2+, the entire circumference of the cell membrane is weakly stained. (C) Score 3+, the entire circumference of the cell membrane is heavily stained. Immunoperoxidase stain, ×200.
Representative cases of pancreatic ductal adenocarcinoma showing scores of 1+ and 2+ for EGFR cytoplasmic expression. (A) Score 1+, faint diffuse cytoplasmic staining is detected. (B) Score 2+, moderate to strong cytoplasmic staining and strong granular staining is observed. Immunoperoxidase stain, ×200.
Clinicopathological characteristics of the patients and tumors.
Surgically resected cancers (n=44)
Far advanced cancers (n=20)
Parameter
n (%)
n (%)
Age (mean ± SD, years)
63.3±3.7
57.3±5.7
<65
23 (52)
13 (65)
≥65
21 (47)
7 (35)
Gender
Male
34 (77)
16 (80)
Female
10 (23)
4 (20)
Tumor site
Head
36 (82)
12 (60)
Body and/or tail
8 (18)
8 (40)
Stage
I
1 (2)
II
32 (73)
III
8 (18)
IV
3 (7)
Grade
1
12 (27)
5 (25)a
2 (10)b
2
28 (64)
3 (15)a
9 (45)b
3
4 (9)
12 (60)a
9 (45)b
Median survival (mean ± SD, month)
24.5±10.3
Primary cancers.
Hepatic metastases. SD, standard deviation.
EGFR immunostaining in the surgically resected cancers and the far advanced cancers obtained at autopsy.
No. of cases (%)
Membranous EGFR reactivity
Cytoplasmic EGFR reactivity
Total
0
1+
2+
3+
0
1+
2+
Surgically resected cancers
44
24 (55)
7 (16)
12 (27)
1 (2)
22 (50)
12 (27)
10 (23)
Far advanced cancers
40
6 (15)
15 (38)
7 (18)
12 (30)
4 (10)
23 (58)
13 (33)
Primary cancersa
20
3 (15)
9 (45)
3 (15)
5 (25)
2 (10)
13 (65)
5 (25)
Hepatic metastasesa
20
3 (15)
6 (30)
4 (20)
7 (35)
2 (10)
10 (50)
8 (40)
No significant difference between membranous and cytoplasmic EGFR reactivity.
Expression of EGFR stratified according to histological grading between the surgically resected cancers and the far advanced cancers obtained at autopsy.
No. of tumors (%)
Histological grade
Total
Membranous EGFR overexpression
P-valuea
Cytoplasmic EGFR overexpression
P-valuea
Surgically resected cancers
44
13 (30)b
10 (23)c
Grade 1
12
1 (8)
0.07
1 (8)
0.2
Grade 2/3
32
12 (38)
9 (28)
Far advanced cancers
40
19 (48)b
13 (33)c
Grade 1
7
3 (43)
0.8
1 (14)
0.3
Grade 2/3
33
16 (48)
12 (36)
P-value indicates comparisons between Grade 1 and Grade 2/3 tumors. No significant difference was noted between EGFR expression and histological grade (Grade 1 vs. 2/3).
P=0.09, statistically significant difference between surgically resected and advanced cancers.
P=0.3, statistically significant difference between surgically resected and advanced cancers.